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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1639312Erstellt: 26. Oktober 2026

Ethyl bromoacetate → Ethyl {3-[(4-bromo-2-fluorophenyl)methyl]-7-chloro-2,4-dioxo-3,4-dihydroquinazolin-1(2H)-yl}acetate

https://huagongshe.com/reaction/1639312

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl bromoacetateHCID 7748—
EduktPotassium CarbonateHCID 11430—
Edukt3-(4-bromo-2-fluorobenzyl)-7-chloro-2,4(1H,3H)-quinazolinedioneHCID 14423799—
LösungsmittelDimethylformamideHCID 6228—
ProduktEthyl {3-[(4-bromo-2-fluorophenyl)methyl]-7-chloro-2,4-dioxo-3,4-dihydroquinazolin-1(2H)-yl}acetateHCID 1143134089,8%

Reaktionsschritte

A solution of 3-(4-bromo-2-fluorobenzyl)-7-chloro-1,2,3,4-tetrahydro-2,4-dioxoquinazoline (500 mg), ethyl bromoacetate (218 mg) and potassium carbonate (360 mg) in N,N-dimethylformamide (5 ml) was stirred at 30° C. for 30 minutes. The solution was evaporated and the residue was dissolved in ethyl acetate. The solution was washed in turn with 0.5N aqueous hydrochloric acid and water, and then dried over magnesium sulfate. The solvent was removed in vacuo to give a crystalline residue, which was crystallized from a mixture of ethyl acetate and n-hexane to give ethyl 2-[3-(4-bromo-2-fluorobenzyl)-7-chloro-1,2,3,4-tetrahydro-2,4-dioxoquinazolin-1-yl]acetate (550 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04883800
Quelldatensatzuspto-grants-1989_11
ORD IDord-da1caf00f70f43c8b47dc88d6a12ba1e
Quellennotizuspto-grants-1989_11